Interleukin-17F gene polymorphisms in Korean patients with Behcet's disease
Interleukin-17F gene polymorphisms in Korean patients with Behcet's disease
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DOI:
10.1007/s00296-008-0664-y
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发表时间:
2008-12-01
影响因子:
4
通讯作者:
Kim, Seong-Kyu
中科院分区:
文献类型:
--
作者:
Jang, Won-Cheoul;Nam, Yun-Hyoung;Kim, Seong-Kyu
IL-17 is a novel cytokine that is characterized by an ability to induce several types of cells to secrete proinflammatory cytokines in various inflammatory diseases. This study analyzed the influence of IL-17F gene polymorphisms on disease susceptibility and clinical features. Ninety-nine Behcet's disease (BD) patients and 114 controls were genotyped to analyze three single nucleotide polymorphisms (SNPs) including A126G, G155A, and A161G of the IL-17F gene using automated sequencing. We compared the frequencies of IL-17F alleles, genotypes, and haplotypes in patients with BD and controls using the chi-square or Fisher's exact test. Significant differences in the frequencies of allele and genotype in A126G SNP of IL-17 gene were found between BD patients and controls (P < 0.001 and P < 0.001, respectively). None of three IL-17F SNPs were associated with diverse clinical features in BD. The frequency of haplotype AA did not differ between patients with BD and controls (P = 0.985). The haplotypes, AG, and GG, have positive and inverse association with BD susceptibility (P < 0.001 and P < 0.001, respectively). These findings suggest that IL-17 gene SNPs may influence the susceptibility of BD.